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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425134Generated: October 27, 2026

Dibromonaphthalic anhydride → Naphthalic anhydride

https://huagongshe.com/reaction/425134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromonaphthalic anhydrideHCID 87118624—
SolventDiethyl EtherHCID 3283—
ProductNaphthalic anhydrideHCID 6693—

Reaction Steps

The following morning thin-layer chromatography showed only a trace presence of the dibromonaphthalic anhydride. The reaction mixture was cooled to room temperature followed by the addition of 350 ml of ether. The triethylamine hydrobromide byproduct was removed by filtration. The filtrate was concentrated on the rotary evaporator, to give the diphenylethynyl derivative of the 1,8-naphthalic anhydride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106142B2
Source datasetuspto-grants-2012_01
ORD IDord-a4c31501d93647848a5dd956a975d0b9
Source noteuspto-grants-2012_01